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Structure of 1256584-73-2
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This boronate moiety integrates seamlessly into Suzuki-Miyaura coupling workflows, offering enhanced reactivity under standard conditions. The para-nitro group facilitates efficient cross-coupling with arylboronic acids, enabling rapid access to complex biaryl architectures in synthetic organic chemistry.
2-(4-Ethyl-3-iodophenyl)-2-methylpropanoic acid serves as a versatile building block for palladium-catalyzed cross-coupling reactions, enabling efficient construction of biaryl and heteroaryl scaffolds. Its sterically hindered α,α-dimethyl carboxylic acid moiety provides excellent bench stability and facilitates straightforward purification. The iodide group exhibits high reactivity in Suzuki, Stille, and Negishi couplings, making this compound ideal for medicinal chemistry campaigns and API intermediate synthesis.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P280-P302+P352
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Lot numbers can be found on the outside label of a product: